MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2018-01-24 for RAINDROP NEAR VISION INLAY 610-0001 RD1-1 manufactured by Revision Optics.
[98163243]
The inlay remains implanted in the patient's eye and is not available for evaluation. The device history record review of the manufacturing lot for this device was performed and there were no discrepancies or unusual findings related to the reported issue. Corneal haze and decreased vision are listed in the device labeling as known potential risks. (b)(4).
Patient Sequence No: 1, Text Type: N, H10
[98163244]
The patient underwent implantation of the raindrop corneal inlay in the left eye on (b)(6) 2017. It should be noted that lasik surgery was performed on this eye concurrent with inlay implantation. On (b)(6) 2017, the patient presented with slight central and superior corneal haze in the operative eye and topical steroids were prescribed. The patient was examined on (b)(6) 2017 at which time his best corrected distance visual acuity (bcdva) decreased from 20/20 (preoperatively) to 20/70-; topical steroids were continued to treat the corneal haze. At last examination on (b)(6) 2018, the corneal haze resolved, bcdva improved to 20/25-2, and the inlay remained implanted. The surgeon believes that concurrent lasik may be a contributing factor.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 3005956347-2018-00016 |
| MDR Report Key | 7217644 |
| Report Source | COMPANY REPRESENTATIVE,HEALTH |
| Date Received | 2018-01-24 |
| Date of Report | 2018-01-24 |
| Date of Event | 2017-11-28 |
| Date Mfgr Received | 2017-12-27 |
| Device Manufacturer Date | 2016-11-22 |
| Date Added to Maude | 2018-01-24 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | MS. PUSHPITA SINGH |
| Manufacturer Street | 25651 ATLANTIC OCEAN DR., STE. A1 |
| Manufacturer City | LAKE FOREST CA 926308835 |
| Manufacturer Country | US |
| Manufacturer Postal | 926308835 |
| Manufacturer Phone | 9497072740 |
| Manufacturer G1 | REVISION OPTICS |
| Manufacturer Street | 25651 ATLANTIC OCEAN DR., STE. A1 |
| Manufacturer City | LAKE FOREST CA 926308835 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 926308835 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | RAINDROP NEAR VISION INLAY |
| Generic Name | CORNEAL INLAY |
| Product Code | LQE |
| Date Received | 2018-01-24 |
| Model Number | 610-0001 |
| Catalog Number | RD1-1 |
| Lot Number | 003045 |
| Device Expiration Date | 2019-11-22 |
| Operator | PHYSICIAN |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | REVISION OPTICS |
| Manufacturer Address | 25651 ATLANTIC OCEAN DR., STE. A1 LAKE FOREST CA 926308835 US 926308835 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2018-01-24 |